FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

88565003: Flexion deformity (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
146847016 Flexion deformity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
831275018 Flexion deformity (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Flexion deformity Is a Deformity true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital overriding toes of left foot (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Talipes calcaneovalgus of bilateral feet (disorder) Associated morphology True Flexion deformity Inferred relationship Some 3
Talipes calcaneovalgus of bilateral feet (disorder) Associated morphology True Flexion deformity Inferred relationship Some 4
An extremely rare chondrodysplastic malformation syndrome characterised by the combination of arachnodactyly, becoming evident at around the age of 10, camptodactyly, and scoliosis. Additional reported manifestations include a mild intellectual disability and a mild facial dysmorphism including a broad nose and flaring nostrils. There have been no further descriptions in the literature since 1972. Associated morphology False Flexion deformity Inferred relationship Some 3
Congenital hammer toe of lesser toe of bilateral feet (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Congenital hammer toe of lesser toe of bilateral feet (disorder) Associated morphology True Flexion deformity Inferred relationship Some 2
Camptodactyly-tall stature-scoliosis-hearing loss syndrome is characterized by camptodactyly, tall stature, scoliosis, and hearing loss (CATSHL). It has been described in around 30 individuals from seven generations of the same family. The syndrome is caused by a missense mutation in the FGFR3 gene, leading to a partial loss of function of the encoded protein, which is a negative regulator of bone growth. Associated morphology False Flexion deformity Inferred relationship Some 1
Camptodactyly syndrome, Guadalajara type 1 is a rare syndrome consisting of growth retardation, facial dysmorphism, camptodactyly and skeletal anomalies. Associated morphology False Flexion deformity Inferred relationship Some 1
Camptodactyly syndrome, Guadalajara type 2 is an extremely rare multiple congenital anomaly syndrome characterized by distinctive intrauterine growth retardation, skeletal dysplasia with multiple malformations including camptodactyly of all fingers, bilateral hallux valgus, short second, fourth and fifth toes, hypoplastic patella, microcephaly, low-set ears, short neck, cuboid-shaped vertebral bodies, pectus excavatum, hip dislocation, and hypoplastic pubic region and genitalia. Camptodactyly syndrome, Guadalajara type 2 has been described in two sisters and is most likely transmitted in an autosomal recessive manner. There have been no further descriptions in the literature since 1985. Associated morphology False Flexion deformity Inferred relationship Some 1
Camptobrachydactyly is an extremely rare brachydactyly syndrome, characterized by short broad hands and feet with brachydactyly associated with congenital flexion contractures of the proximal and/or distal interphalangeal joints of the fingers, as well as syndactyly of feet. Polydactyly, septate vagina and urinary incontinence were also occasionally reported. Camptobrachydactyly has been described in 18 members of 1 family, suggesting an autosomal dominant inheritance. There have been no further descriptions in the literature since 1972. Associated morphology False Flexion deformity Inferred relationship Some 2
Correction of camptodactyly Direct morphology False Flexion deformity Inferred relationship Some 1
A congenital malformation syndrome with the association of a permanent camptodactyly of the fingers and the over excretion of taurine in the urine. Camptodactyly mainly affects the little finger, although any finger may be involved. The disease has been described in 17 affected patients from 4 unrelated families. An autosomal dominant inheritance has been suggested. There have been no further descriptions in the literature since 1966. Associated morphology False Flexion deformity Inferred relationship Some 1
Congenital hyperflexion of limb Associated morphology True Flexion deformity Inferred relationship Some 1
Thumb in palm deformity Associated morphology True Flexion deformity Inferred relationship Some 1
Swan-neck deformity of finger of bilateral hands Associated morphology True Flexion deformity Inferred relationship Some 2
Swan-neck deformity of finger of bilateral hands Associated morphology True Flexion deformity Inferred relationship Some 4
A rare, genetic developmental defect during embryogenesis syndrome characterized by camptodactyly, joint contractures with amyotrophy, and ectodermal anomalies (oligodontia, enamel abnormalities, longitudinally broken nails, hypohidrotic skin with tendency to excessive bruising and scarring after injuries and scratching), as well as growth retardation, kyphoscoliosis, mild facial dysmorphism, and microcephaly. There have been no further descriptions in the literature since 1992. Associated morphology False Flexion deformity Inferred relationship Some 5
Camptobrachydactyly is an extremely rare brachydactyly syndrome, characterized by short broad hands and feet with brachydactyly associated with congenital flexion contractures of the proximal and/or distal interphalangeal joints of the fingers, as well as syndactyly of feet. Polydactyly, septate vagina and urinary incontinence were also occasionally reported. Camptobrachydactyly has been described in 18 members of 1 family, suggesting an autosomal dominant inheritance. There have been no further descriptions in the literature since 1972. Associated morphology False Flexion deformity Inferred relationship Some 5
A rare, genetic, congenital limb malformation syndrome characterised by a unique combination of bilateral, symmetrical camptodactyly and clinodactyly of 5th fingers, mesoaxial camptodactyly of toes, and ulnar deviation of 3rd fingers. Additional variable manifestations include bifid toes and severe syndactyly, or synpolydactyly, involving all digits of hands and feet. Associated morphology False Flexion deformity Inferred relationship Some 3
Acquired calcaneovalgus deformity of right foot Associated morphology True Flexion deformity Inferred relationship Some 3
Acquired calcaneovalgus deformity of bilateral feet Associated morphology True Flexion deformity Inferred relationship Some 6
Acquired calcaneovalgus deformity of bilateral feet Associated morphology True Flexion deformity Inferred relationship Some 5
Acquired calcaneovalgus deformity of left foot Associated morphology True Flexion deformity Inferred relationship Some 3
Congenital crossed toes Associated morphology True Flexion deformity Inferred relationship Some 2
Postural calcaneovalgus Associated morphology True Flexion deformity Inferred relationship Some 2
Calcaneovalgus deformity of foot Associated morphology True Flexion deformity Inferred relationship Some 3
Fixed flexion deformity (morphologic abnormality) Is a True Flexion deformity Inferred relationship Some
Acquired overriding toe Associated morphology True Flexion deformity Inferred relationship Some 2
A rare, genetic developmental defect during embryogenesis syndrome characterized by camptodactyly, joint contractures with amyotrophy, and ectodermal anomalies (oligodontia, enamel abnormalities, longitudinally broken nails, hypohidrotic skin with tendency to excessive bruising and scarring after injuries and scratching), as well as growth retardation, kyphoscoliosis, mild facial dysmorphism, and microcephaly. There have been no further descriptions in the literature since 1992. Associated morphology False Flexion deformity Inferred relationship Some 9
Flexion deformity of joint of bilateral ankles (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of bilateral ankles (disorder) Associated morphology True Flexion deformity Inferred relationship Some 2
Flexion deformity of joint of right ankle Associated morphology True Flexion deformity Inferred relationship Some 1
Bilateral flexion deformity of elbow joints Associated morphology True Flexion deformity Inferred relationship Some 1
Bilateral flexion deformity of elbow joints Associated morphology True Flexion deformity Inferred relationship Some 2
Flexion deformity of joint of left ankle (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of left elbow (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of right elbow Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of right foot Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of left foot Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of right wrist Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of left wrist (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of right knee (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of left knee (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of bilateral shoulder regions (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of bilateral shoulder regions (disorder) Associated morphology True Flexion deformity Inferred relationship Some 2
Talipes calcaneovarus of bilateral ankles and feet (disorder) Associated morphology True Flexion deformity Inferred relationship Some 3
Talipes calcaneovarus of bilateral ankles and feet (disorder) Associated morphology True Flexion deformity Inferred relationship Some 4
Congenital talipes calcaneovalgus Associated morphology True Flexion deformity Inferred relationship Some 3
Congenital mallet toe (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Acquired right mallet toe (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Acquired left mallet toe (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Acquired bilateral mallet toe (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Acquired bilateral mallet toe (disorder) Associated morphology True Flexion deformity Inferred relationship Some 2
Acquired mallet toe (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of left shoulder region (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of left hip Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of right hip (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of bilateral hips (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of bilateral hips (disorder) Associated morphology True Flexion deformity Inferred relationship Some 2
Flexion deformity of joint of bilateral wrist regions (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of bilateral wrist regions (disorder) Associated morphology True Flexion deformity Inferred relationship Some 2
Flexion deformity of joint of right shoulder region (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Bilateral flexion deformity of knees Associated morphology True Flexion deformity Inferred relationship Some 1
Bilateral flexion deformity of knees Associated morphology True Flexion deformity Inferred relationship Some 2
Flexion deformity of joint of bilateral feet (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Flexion deformity of joint of bilateral feet (disorder) Associated morphology True Flexion deformity Inferred relationship Some 2
Dorsiflexion deformity of foot Associated morphology False Flexion deformity Inferred relationship Some 1
Bilateral acquired calcaneovarus deformity of feet Associated morphology True Flexion deformity Inferred relationship Some 3
Bilateral acquired calcaneovarus deformity of feet Associated morphology True Flexion deformity Inferred relationship Some 4
Acquired hammer toe of lesser toe of left foot (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Acquired hammer toe of lesser toe of right foot (disorder) Associated morphology True Flexion deformity Inferred relationship Some 1
Dorsiflexion deformity (morphologic abnormality) Is a True Flexion deformity Inferred relationship Some

Start Page 2 of 2

This concept is not in any reference sets

Back to Start